Methods for engineering t-cell receptors

a technology of t-cell receptors and engineering methods, which is applied in the field of methods for engineering t-cell receptors, can solve the problems that the grafting of cdr-loops into structural loop regions of variable domains has not been demonstrated to allow engineering of bispecific molecules

Inactive Publication Date: 2013-02-14
F STAR BIOTECHNOLOGISCHE FORSCHUNGS & ENTWICKLUNGS GMBH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0046]Said T-cell receptor domain polypeptide can preferably bind to an epitope of an antigen, for example serum proteins, Fc-receptors, complement molecules and serum albumins. Binding to these antigens can be advantageous as native TCRs do not have any effector functions. By developing modified T-cell receptor domain polypeptides binding Fc receptors like Fc gamma I, II or III or neonatal Fc receptors or complement proteins, TCRs can be obtained having effector function capabilities. Alternatively, also serum half lifesof the so modified TCRs due to binding to neonatal Fc receptors can be increased if appropriate. This can be especially highly advantageous for therapeutic purposes.

Problems solved by technology

However, it is doubtful that the relative orientation of the CDR-loops and the structural loops is similar in sufficient detail and resolution; consequently it has not been described to date that it is actually possible to develop bispecific molecules by this technique.
Fusion proteins, however, are frequently difficult to produce and may lead to enhanced immunogenicity if the molecule is used therapeutically.
Grafting of CDR-loops into structural loop regions of variable domains has not been demonstrated to allow for engineering of bispecific molecules.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

[0219]A number of different libraries are constructed based on a soluble version of the 1G4 TCR, which is specific for the NY-ESO epitope (WO2605113595).

[0220]The library genes are assembled from specific synthetic oligonucleotides and cloned as full length TCR alpha and beta chains displayed on filamentous phage. The alpha chain is expressed in soluble format, and the beta chain is expressed as in-frame fusion to the geneIII coat protein of M13 bacteriophage. The alpha chain has a non-native Cystein residue (encoded by the mutation Thr84Cys (IMGT numbering)) and the beta chain has a non-native Cystein residue (encoded by the mutation Ser79Cys (IMGT numbering)) to allow heterodimer formation. Cloning, selection and characterization can be done as described in Li et al. (2005) Nat. Biotechnol. 23:349-354. The following 1G4 TCR gene and library gene pairs are cloned into the three-cistron phage display vector, pEX746 essentially as described in Li et al. (2005) Nat. Biotechnol. 23:349...

example 2

[0244]After ligation of the library inserts into the vector, the steps of phage preparation are performed following standard protocols. Briefly, the ligation mixtures are transformed into, E. coli TGA cells by electroporation. Subsequently, phage particles are rescued from E. coli TG1 cells with helper phage M13-KO7. Phage particles are then precipitated from culture supernatant with PEG / NaCl in 2 steps, dissolved in water and used for selection by panning or, alternatively, they were stored at minus 80° C. Selection of clones binding specifically to Human serum albumin:

[0245]The libraries as described in example 1 are used in panning rounds for the isolation of specifically binding clones following standard protocols. Briefly, the phage libraries are suspended in binding buffer (PBS, 1% ovalbumin, 0.005% Tween 20) and panned against human serum albumin immobilized directly on maxisorp plates (10 micrograms / ml in PBS, overnight at 4° C.; plates are blocked with Blocker Casein (Pierc...

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Abstract

The present invention provides a method for engineering a T-cell receptor domain polypeptide comprising at least one modification in a structural loop region of the T-cell receptor domain polypeptide and determining the binding of the T-cell receptor domain polypeptide to an epitope of an antigen, wherein the unmodified T-cell receptor domain polypeptide does not significantly bind to said epitope. The present invention also covers modified T cell receptor domain polypeptides, their use and libraries containing the modified T cell receptor domain polypeptides.

Description

[0001]This application is a continuation of U.S. Ser. No. 12 / 307,582, filed Sep. 14, 2009, which is a 371 national stage entry of PCT / AT2007 / 000342, filed Jul. 5, 2007, which claims the benefit of Austrian patent application A1146 / 2006 filed Jul. 5, 2006; each of these applications are incorporated by reference herein in their entirety.FIELD OF INVENTION[0002]The present invention relates to a novel method for engineering and manufacturing of modified T-cell receptors and T-cell receptor domain polypeptides with the aim to impart them with specific binding properties. Further, modified T-cell receptor domain polypeptides obtained by said method and their use for establishing libraries and developing detection and screening methods for possible binding structures are disclosed.BACKGROUND[0003]T-cell receptors (TCRs) are important molecules of the immune system. Its extracellular domains are homologous with and structurally similar to an antibody Fab fragment.[0004]T-cell receptors ar...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07K14/725C40B30/04G01N33/566C40B40/10C07K1/107C12N15/12
CPCC07K14/7051
Inventor HIMMLER, GOTTFRIEDRUKER, FLORIAN
Owner F STAR BIOTECHNOLOGISCHE FORSCHUNGS & ENTWICKLUNGS GMBH
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